HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-4-methoxypyridine-N-oxide → (4-methoxypyridin-2-yl)methyl Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-4-methoxypyridine-N-oxide | HCID 10701893 | — |
| Reactant | 2-Acetoxymethyl-6-chloropyridine | HCID 10726190 | — |
| Product | (4-methoxypyridin-2-yl)methyl Acetate | HCID 10726082 | — |
Reaction Steps
Starting with 2-methyl-4-methoxypyridine-1-oxide (2.1 g) in the procedure of Part (ii) afforded 2.5 g of 2-acetoxymethyl-4-methoxypyridine which was contaminated with about 25% of 5-acetoxy-2-methyl-4-methoxypyridine. This mixture was dissolved in methanol (10 ml) containing 1.118 g (20.7 mmole) sodium methoxide and stirred at reflux for one hour. The methanol was evaporated in vacuo, the residue diluted with water, neutralized with dilute hydrochloric acid and extracted with chloroform. The organic layer was washed with brine, dried (MgSO4) and concentrated in vacuo to give 853 mg (41%) 2-hydroxymethyl-4-methoxypyridine. 1H-NMR(CDCl3)ppm (delta): 3.9 (s, 3H), 4.72 (s, 2H), 5.35 (bs, 1H), 6.7 (dd, 1H), 6.95 (d, 1H), 8.3 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05015473 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-4df8e2fc6e9148b58a384d43c71a5c6e |
| Source note | uspto-grants-1991_05 |